Variant report

Variant rs4148601
Chromosome Location chr11:17494062-17494063
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:17461200-17497400 Weak transcription Gastric stomach
2 chr11:17465800-17496400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr11:17480200-17494200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr11:17480200-17494800 Weak transcription H9 Cell Line embryonic stem cell
5 chr11:17481800-17495200 Weak transcription Brain Hippocampus Middle brain
6 chr11:17487200-17494200 Weak transcription Brain Inferior Temporal Lobe brain
7 chr11:17490200-17496200 Weak transcription Brain Germinal Matrix brain
8 chr11:17492000-17495200 Weak transcription Brain Angular Gyrus brain
9 chr11:17492000-17497200 Weak transcription Fetal Brain Female brain
10 chr11:17492800-17494400 Weak transcription Spleen Spleen
11 chr11:17493200-17496400 Weak transcription Brain Anterior Caudate brain
12 chr11:17493600-17494200 Enhancers Pancreatic Islets Pancreatic Islet
13 chr11:17494000-17494200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr11:17494000-17495400 Enhancers ES-UCSF4 Cell Line embryonic stem cell

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